Canonical Allele Identifier: CA2954899284

Gene: SYP

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.49191402T>C , CM000685.2:g.49191402T>C	GRCh38
NC_000023.10:g.49047859T>C , CM000685.1:g.49047859T>C	GRCh37
NC_000023.9:g.48934803T>C	NCBI36
NG_012532.1:g.13803A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689634.1:n.2564A>G
ENST00000692723.1:n.972+31A>G
ENST00000263233.9:c.*4+31A>G MANE Select	ENSP00000263233.4:n.*4+31A>G
ENST00000263233.8:c.*4+31A>G	ENSP00000263233.4:n.*4+31A>G
ENST00000376303.6:c.*698+31A>G	ENSP00000365480.2:n.*698+31A>G
ENST00000472598.5:c.615+31A>G
ENST00000479808.5:c.*35A>G	ENSP00000418169.1:n.*35A>G
NM_003179.2:c.*4+31A>G	NP_003170.1:n.*4+31A>G
XM_011543950.1:c.*4+31A>G	XP_011542252.1:n.*4+31A>G
XM_011543951.1:c.*4+31A>G	XP_011542253.1:n.*4+31A>G
NM_003179.3:c.*4+31A>G MANE Select	NP_003170.1:n.*4+31A>G